Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into… — Class II medical device recall Z-2039-2024
Completed recall by Mckesson Medical-Surgical Inc. Corporate Office, reported 2024-06-19, distributed nationwide. Quarantined product was inadvertently distributed
| Recall number | Z-2039-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mckesson Medical-Surgical Inc. Corporate Office, Richmond, VA, United States |
| Recall initiated | 2024-04-23 |
| Classified | 2024-06-07 |
| Reported by FDA | 2024-06-19 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 20884521012230 |
| Lot numbers | 330737X |
| Model numbers | 1159851, 8881560125 |
Product
Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into or withdraw fluids from the body MMS Catalog Number: 1159851 Cardinal Catalog Number: 8881560125
Reason for recall
Quarantined product was inadvertently distributed
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2039-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.